Compositions and methods for activation and overexpression of secondary metabolites in microorganisms

ABSTRACT

Methods and compositions herein provide non-naturally occurring γ-butyrolactones (GBLs) in racemic mixtures that increase efficiency and effectiveness of screening for production of antibiotics, and enhance yields and express silent pathways. Non-naturally occurring GBLs were synthesized and found to stimulate antibiotic production in several different streptomycete strains. Antibiotic production by  Streptomyces coelicolor  was induced by a racemic mixture of non-cognate stereoisomers of VB-D, seven of which are non-naturally occurring. Further, novel A-factor-type GBL analogs stimulated antibiotic production in  S. coelicolor . Synthesis in response to the treatment with the non-cognates GBL was observed for known compounds including undecylprodigiosin, desferrioxamine and streptorubin B, as was synthesis of a compound of unknown structure. A group of  37  additional microbial strains was screened by principal component analysis to determine optimal concentrations of each of a panel of four non-cognate synthetic GBLs for addition to cultures with optimal stimulation of secondary metabolites, and large scale fermentations were analyzed and product enhancement by the GBLs was observed.

RELATED APPLICATION

The present application claims the benefit of U.S. provisionalapplication Ser. No. 62/292,952 filed Feb. 9, 2016, entitled“Compositions and methods of activation and overexpression of secondarymetabolic gene clusters in microorganisms”, inventors Dakota BenjaminHamill and Jake J. Cotter, and which is hereby incorporated herein inits entirety.

TECHNICAL FIELD

Methods and compositions are provided herein to activate inmicroorganisms secondary metabolic pathways that are silent or underexpressed in laboratory conditions, and to identify and overexpressbioactive compounds and to discover products of silent pathways.

BACKGROUND

The number of new classes of antibiotics discovered over the past 25years has been decreasing due to inefficiencies in the process ofantibiotic discovery. See, Silver, L.; Expert Opin. Drug Discovery,3(5): 487-500; Silver, Future Microbiol., 10(11): 1711-1718 (2015). Infact, no major classes of antibiotics have been introduced between 1962and 2000. The most recently introduced antibiotic classes: linezolid,daptomycin, and retapamulin, were introduced in 2000, 2003, and 2007,respectively. These chemical classes: pleuromutilins, oxazolidinones,and acid lipopeptides, were first reported or patented in 1952, 1978,and 1987, respectively. See, Silver, Clinical Microbiology Reviews,24(1):71-109 (2011). Antibiotic resistance has increased steadily duringthe same time period that antibiotic discovery has slowed. Antibioticresistance is commonly the result of horizontal gene transfer anddevelops from environmental pressures. See, Silver, Future Microbiol.,10(11): 1711-1718 (2015).

In the 1950s, about 1,000 soil microbes were generally required to beisolated to be screened to find a new antibiotic. More than 10,000,000soil microbes were required by the 1980s to be isolated and screened forthe industry to produce a new antibiotic. The research approach was toscreen more samples, instead of building tools to screen moreeffectively. This has led to a cost ineffective business model thatresulted in decline of antibiotic discoveries during recent decades. Forexample, the actinomycete family of a soil bacteria, was previously themost important sources for antibiotics, yet these microorganisms havebeen nearly abandoned in recent years in favor of high-throughput targetbased screening of chemical libraries because of the lack of successwith prior methods of discovery. See, Baltz, Current Opinion inPharmacology, 8(5):557-563 (2008).

A small percentage of secondary metabolic pathways are thought to beactive under laboratory culture conditions. See, Epstein, Science296.5570: 1127-1129 (2002). Silent gene clusters and under expressedsecondary metabolic gene clusters produce undetectable levels ofbioactive compounds under laboratory conditions of culture andscreening. Traditional laboratory techniques for bioactive compoundscreening include using fermentation broths for detection. See, Silver,Future Microbiol., 10(11): 1711-1718 (2015). This approach has beenlargely abandoned in favor of hypersensitive screening methods such asgenomic strategies for activating known operons and pathways, forexample, reporter strains screening, synergy screening, and antisensescreening. Ibid. Few microorganisms from environmental samples producebioactive compounds on known solid media in Petri dishes or in broth orliquid cultures due to absence of environmental signals that typicallytake place in the native community of the microorganism. Previousattempts to assemble these gene clusters in vitro for exogenousexpression have been largely unsuccessful. Methods of gaining access tothese pathways are clearly desirable. Such methods would transformmicrobiology and the healthcare system by accelerating drug discovery.

Streptomyces bacteria are a large family of Gram-positive actinomycetes,cells of which have an ensemble of biosynthetic pathways that generatesmall molecules with potent biological activities against otherorganisms including about 70% of antibiotics currently clinically usedand drugs to treat other diseases such as fungal infections and cancer.See, Nodwell, Molecular Microbiology, 94(3): 483-485 (2014). Secondarymetabolites have evolved to repel or attract other organisms as asurvival mechanism. See, Silver L., Expert Opin. Drug Discovery, 3(5):487-500 (2008).

Gamma (γ)-butyrolactones (GBLs) are an important family of signalingmolecules that regulate antibiotic production. See, Nodwell, MolecularMicrobiology, 94(3): 483-485 (2014). For example, antibioticdaunorubicin in Streptomyces peucetius, streptomycin in Streptomycesgricseus, virginiamycin in Streptomyces virginae, actinorhodin inStreptomyces coelicolor, undecylprodigiosin in S. coelicolor, andlankamycin in Streptomyces violaceceoniger are regulated by GBLsignaling, and structures of these antibiotics are provided in FIG. 4 .Structures of 14 known naturally occurring GBLs are shown in FIG. 5 .

Most GBLs are produced in minute quantities. The biosynthetic pathwaysthat regulate antibiotic production using GBLs as a primaryintercellular signal are diverse. See, Biarnes-Carrera et al., CurrentOpinion in Chemical Biology, 28:91-98 (2015). At least fourteennaturally occurring GBLs have been characterized, and are classifiedinto groups: A-factor with 1′-keto group, which is the most common GBLused in research; virginiae butanolide (VB) with a 1′-α-hydroxyl; andIM-2 with a 1′-β-hydroxyl. See, Hsiao et al., Chemistry & Biology, 16:951-960 (2009); Biarnes-Carrera et al., Current Opinion in ChemicalBiology, 28: 91-98 (2015). A-factor was first characterized as anendogenously produced hormone that controls a gene cluster involved insporulation and secondary metabolism in Streptomyces griseus. See, Hsiaoet al., Chemistry & Biology, 16: 951-960 (2009). GBLs generally havespecific and sensitive receptors. See, Biarnes-Carrera et al., CurrentOpinion in Chemical Biology, 28: 91-98 (2015). The specificity wasdemonstrated by the observation that A-factor analogs with one extracarbon or with fewer than eight carbons had a 10-fold lower activitythan naturally occurring A-factor. See, Hsiao et al., Chemistry &Biology, 16: 951-960 (2009).

The number of antibiotics approved by the Food and Drug Administrationhas decreased from 16 in 1983-1987 to 2 in 2008-2012, see FIG. 1 . Asantibiotic resistance has sharply increased during this period, the needfor new antibiotics has become more urgent.

SUMMARY

An aspect of the invention herein provides a composition forupregulating biosynthesis and production of a bioactive microbialproduct by cells of a sample of microorganisms, the compositionincluding:

-   -   at least one synthetic non-naturally occurring derivative of a        γ-butyrolactone (GBL) core, in a dose effective to increase        expression of the genes and biosynthetic production of the        product in the cells.

In an embodiment of the composition, the bioactive product has at leastone activity selected from the group consisting of: anti-bacterial,anti-fungal, anti-viral, anti-helminthic, anti-cancer, anti-malarial,anti-trypanosomal, complement inhibitory, anti-spasmodic, toxinneutralizing, immune stimulant, anti-inflammatory, immune suppressant,diuretic, and herbicidal.

In certain embodiments of the composition, the sample of themicroorganisms is a mixture of a plurality of strains or species, andthe composition is effective to upregulate expression of genes in atleast one of the strains or species. In an embodiment of thecomposition, the synthetic non-naturally occurring derivative of the GBLhas a chemical structure different from naturally occurring GBLs, andthe composition structure does not have the same as: Streptomycesgriseus A-factor; S. viridochrornogenes Factor I; S. lavendulae IM-2; S.coelicolor SCB1, SCB2, and SCB3; anthracyclines from S.bikiensis; S.cyaneofuscatus greater length hydrocarbon chains in 2R3R and 2S3S; andS.virginiae butanolides VB-A, VB-B, VB-C, VB-D, and VB-E. The term“non-naturally occurring” as used herein means a GBL having a chemicalstructure which is not found in nature, or is a stereoisomer or anenantiomer of a naturally produced GBL which is not found in nature.

In certain embodiments of the composition, the GBL comprises a corewhich is substituted at the 3 position by a group having the structuremethyl-R₁ and at the 2 position by a group having the structure selectedfrom ketone-R_(2,) alcohol-R_(2,) and carbonyl-R₂, wherein thesubstituent at the 2 and 3 position of the GBL are attached to the GBLcore by recto (R) or levo (L) bonds, wherein R₁ and R₂ are eachindependently selected from the group consisting of: a lower alkane, analkyne, an alkoxyl, an alkoxy, a halogen, a sulfide, an amine, acarbonyl, and an alkene selected from the group consisting of: an ethyl,an ethoxy, an ethoxyl, a propyl, a propoxy, a propoxyl, a butyl, apentyl, a hexyl, a t-butyl, an s-butyl, an i-butyl, an i-pentyl, ani-hexyl, and an i-heptyl.

In an embodiment of the composition, the GBL core is substituted at the2 or 3 position with a lower alkane having a length of 1 carbon to about8 carbons. In certain embodiments of the composition, the GBL core issubstituted at the 2 or 3 position with an alkane having a lengthgreater than 8 carbons. In an embodiment of the composition, the R₁includes hydroxyl and is either recto-(R) or levo-(L), and R₂ comprisesa hexyl which is R or

L. In certain embodiments the composition is selected from at least oneenantiomer or stereoisomer of the group consisting of3-(1-hydroxyethyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one;3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one;3-acetyl-4-(hydroxymethyl)dihydrofuran-2(3H)-one; and,3-heptanoyl-4-(hydroxymethyl)dihydrofuran-2(3H)-one.

An aspect of the invention herein provides a method of improving a yieldof a microbially-produced bioactive secondary metabolite product, themethod including

-   -   contacting cells of at least one strain of microorganism with a        suitable amount of at least one γ-butyrolactone (GBL)        composition such that the GBL is non-cognate to the strain or is        synthetic and non-naturally occurring, and culturing the cells        of the strain with the GBL under conditions for production of        the product; and,    -   obtaining the product from the cells by separation of cells and        medium or purification of the product from the cells and        analyzing the amount of the product, and determining that the        yield of the product per unit of volume of culture or the yield        of the product per weight of cells is greater than that from        control cells of the strain not so contacted with the GBL        composition and otherwise identically cultured and analyzed, and        therefore the yield of the product from the cells cultured with        the derivative of the GBL is improved compared to that from the        control cells.

In an embodiment of the method, the strain of microorganism isbacterial. In certain embodiments of the method, the strain of bacteriais an actinomycete. In an embodiment of the method, the strain ofmicroorganism is fungal or algal. In certain embodiments of the method,the derivative of the GBL is synthetic and non-naturally occurring andis at least one of the compositions selected from formulas I-VII in FIG.10 . In an embodiment of the method, a genus of the actinomyceteselected from the group of genera consisting of: Actinopolyspora,Amycolatopsis, Micromonospora, Nocardia, Pseudonocardia, Saccharothrix,Saccharopolyspora, Salinospora, Streptomyces, Tetinomedara, andVerrucosispora. In certain embodiments of the method, the yield of theproduct from the cells contacted with the GBL is at least about two-foldgreat, four-fold great, ten-fold greater, or at least about twenty-foldgreater than from the control cells. In certain embodiments of themethod, the genus is Streptomyces and the species is selected from atleast one of the group consisting of: avermitilis, S. aureofaciens, S.capreolus, S. cattleya, S. clavuligerus, S. coelicolor, S. fradiae, S.garyphallus, S. griseus, S. kanamyceticus, S. levoris, S. lincolnensis,S. niveus, S. noursei, S. platensis, S. plicatus, S. pristinaespiralis,S. orientalis, S. ribosidifus, S. rimosus, S. roseosporus, S. scabiei,S. venezuelae, S. vinaceus, and S. virginiae; or the genus is at leastone Pseudonocardia species selected from the group of: P. acacia; P.ailaonensis; P. adelaidensis; P. alaniniphila; P. ammonioxydans; P.carboxydivorans; P. halophobia; P. kujensis; P. nitrificans; P.petroleophila; P. salarnisensis; P. sulfoxidans; P. thermophila; and P.zigingensis; or the genus is Amycolatopsis and the species is at leastone selected from the group of: A. alba, A. azurea, S. balhimycena, A.coloradensis, A. fastidiosa, A. keratiniphila, A. lurida, A.mediterranei, A. orientalis, A. sulphurea, A. tolypomycina, and A.vancoresmycina.

An aspect of the invention herein provides a method of discovery of acell-produced secondary metabolic compound in a microbial straincontaining putative unexpressed or under expressed genes encodingenzymes for biosynthesis of a chemical entity having a medicinal orindustrial biological activity, the method including:

-   -   contacting cell samples containing cells from at least one        microbial strain with at least one synthetic non-naturally        occurring or non-cognate γ-butyrolactone (GBL) in an amount        suitable for inducing secondary metabolite expression, such that        the microbial strains are selected from the group of: fresh        isolates from nature, a naturally occurring mixture of        unpurified microorganisms, and an established species strain        wherein the GBL and the established species are non-cognate;    -   culturing the cell samples with the GBL under conditions for        production of the secondary metabolite chemical compounds;    -   screening the cultures by at least one detection system for        presence of the biological activity, or by at least one        detection system for presence of the metabolite not so expressed        in control samples not contacted with the GBL and otherwise        identical and further screening the metabolite for the        biological activity, and the presence of the biological activity        identifies the producing sample containing at least one strain        of microorganism producing the chemical having the activity;        and,    -   characterizing at least one chemical structure having the        biological activity, and comparing the structure to a library        database of known chemical entities to obtain chemicals not        previously known, thereby screening to discover the chemical        compounds with the biological activity. In an embodiment of the        method, the at least one microbial strain contains at least two,        at least five, or at least 10 strains. In certain embodiments of        the method, the GBL is a plurality of GBLs having non-identical        chemical structures, and the plurality is at least two or at        least five GBLs. In an embodiment of the method, the        non-identical chemical structure includes a GBL which is a        racemate, enantiomer, stereoisomer, or a racemic mixture. In        certain embodiments of the method, screening further includes        contacting each of the samples to the detection system for the        biological activity, the detection system including at least one        component selected from the group of: an enzyme, an organism, a        tissue culture, a cell culture; the method further including        measuring an activity selected from: antibacterial; antifungal;        herbicidal; anti-helminthic; insecticidal; anti-viral; an        anti-cancer; immune suppressant; anti-inflammatory; and        anti-spasmodic. In an embodiment of the method, culturing cell        samples is in a liquid medium, and the method further includes        prior to screening, separating the cells from the medium to        obtain a resulting supernatant depleted of the cells and a        resulting cell pellet. In certain embodiments of the method,        culturing cell samples is in contact with soil, and the method        further includes prior to screening, separating the cells from        the soil and washing the soil and cells, to obtain resulting        components of supernatant, cell pellet, and soil, and assaying        each for amount of the biological activity.

An embodiment of the method further includes after identifying,isolating the chemical compound from the producing culture contactedwith the GBL. An embodiment of the method further includes isolating,from the plurality of GBLs contacted to the sample, the at least one GBLthat induces expression of the product.

In an embodiment of the method, characterizing the chemical structurefurther includes analyzing by at least one method selected from thegroup consisting of: mass spectrometry (MS); gas chromatography; thinlayer chromatography; matrix-assisted laser desorption/ionization(MALDI); MALDI-time of flight (MALDI-TOF); moving bed chromatography;and high performance liquid chromatography (HPLC). In certainembodiments of the method, culturing is growing the strain or strains onsolid medium, and screening further includes adding cells of a targetindicator strain comprising at least one of a bacterium, a fungus, aeukaryotic cell, a white blood cell, and a eukaryotic tissue explant. Anembodiment of the method further includes testing a sample of thesupernatant in a test subject, which is an experimental animal model ofa disease.

An embodiment of the method further includes testing a sample of thesupernatant in vivo in cultured cells or tissues of an organism selectedfrom the group consisting of: a mammal; a fungus; a helminth; a plant;and, an insect.

An embodiment of the method further includes obtaining coordinates ofpeaks observed by MS, MALDI, MALDI-TOF, or HPLC corresponding topresence of secondary metabolism products, and comparing the location ofthe peaks to that of known previously characterized products to identifychemical entities, and further to characterize products from databasesas previously identified chemicals, or as potentially novel chemicalentities. An embodiment of the method further includes isolating andscreening the cell sample strains for production of the novel chemicalentities in presence of the GBL.

An aspect of the invention herein provides a method of increasing oraccelerating production of a microbial secondary metabolism compound bya producing microorganism, the method including:

-   -   contacting a culture of the producing microorganism strain with        a GBL at an effective dose to upregulate expression and        production of the compound, for example, by inducing or by        derepressing operons of genes encoding enzymes that synthesize        the compound, or by inactivating inhibitors of expression, such        that the GBL is non-cognate to the strain or is a non-naturally        occurring GBL. In certain embodiments, the GBL is added at or        before inoculation of production culture medium cells of the        strain. In an alternative embodiment of the method, the GBL is        added after inoculation or during growth of cells of the strain.        In another alternative embodiments of the method, the GBL is        added at stationary phase or after cessation of growth of the        cells of the strain. In another alternative embodiment of the        method, the GBL is added at a plurality of time points during        culture of the micro-organism.

An embodiment of the method further includes comparing amount of thesecondary metabolism compound with that of a control culture notcontacted with the GBL and otherwise identical. In an embodiment of themethod, the effective dose of the GBL is about 0.2 μM-0.8 μM, 0.8 μ-20μM, 20 μM-100 μM, or is greater than 100 μM.

An embodiment of the invention provides a novel chemical produced by aculture of S. coelicolor treated with at least one enantiomer orstereoisomer of3-(1-hydroxyheptyl)-4-(hydroxymethyl)Dihydrofuran-2(3H)-one, and elutingfrom a mass spec time of flight analysis with a peak at 1.84.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a bar graph of number of antibiotics approved in four yearintervals from 1983-2012, and appearance of organisms with antibioticresistance during this period. The line indicates increased incidence ofresistance to antibiotics during this period.

FIG. 2 is a photograph of each of an untreated control plate culture ofS. coelicolor strain A3(2) and a plate culture of S. coelicolor that wastreated by depositing a 2 μL volume of a solution of a racemic mixturecontaining 165 μg of non-naturally occurring A-factor type GBLsindicated herein as X and XI (see, Example 6 and FIG. 8 ). The dark areaon the treated plate indicates production of the purple antibiotic,actinorhodin.

FIG. 3 is a photograph of culture plates containing S. coelicolor as inFIG. 2 arranged as a function of increasing amount of GBL contacted toeach plate from left to right showing actinorhodin production. Thefigure shows a dose-dependent increase in antibiotic production from S.coelicolor in response to increased GBL concentration contacted on thesuccessive plates.

FIG. 4 is an illustration of structures of six antibiotics that areregulated by GBL signaling and the names of the producing strains ofStreptomyces.

FIG. 5 is an illustration of the structures of 14 known members of theGBL class of signaling molecules that regulate antibiotic production anddifferentiation, and the names of the cognate species in whichproduction is regulated.

FIG. 6 is an illustration of the organic synthesis of the GBLs of thecompositions and methods herein.

FIG. 7 is a photograph of plate cultures of S. coelicolor. The fourplates in the top row are negative control plates receiving an aliquotof vehicle only, and that were not contacted with GBLs, showing that thevehicle affects neither growth nor antibiotic production. The plates inrows 2-6 were contacted with a racemic mixture of synthetic A-factortype GBLs indicated herein as X and XI as shown in FIG. 8 .

FIG. 8 is a drawing of the structures of non-naturally occurring GBLsand indicated herein as X and XI.

FIG. 9 is a photograph of control plate cultures (top row) of S.coelicolor contacted with vehicle, and experimental plate cultures of S.coelicolor contacted with a racemic mixture of VB-D and seven enantiomerGBLs thereof having the formulas I-VII (see, FIG. 10 ). The dark area onthe plates indicates production of the blue antibiotic, actinorhodin,and red prodiginies. A monotonic dose-dependent response of antibioticproduction (diameter of dark spot) as a function of amount of GBLmixture was observed.

FIG. 10 is an illustration of the structures of non-naturally occurringenantiomeric GBLs named herein as I-VII, and the structure of naturallyoccurring VB-D.

FIG. 11 is an illustration of the structures of potential functionalgroups to use to synthesize novel GBL derivatives to screen to determineactivity to induce antibiotic production.

FIG. 12 is a photograph of the plates of FIG. 7 that yielded a positiveeffect, viz., actinorhodin production, arranged in order of increasingGBL dose from left to right.

FIG. 13 is an illustration non-naturally occurring analogs of A-factortype, VB type, and SCB type of GBLs and acylated homoserine lactones(AHLs) for synthesis and testing for activity to induce antibioticproduction.

FIG. 14A-C are photographs of thin-layer chromatograms (TLC) comparingresults of the butenolide formation step shown in FIG. 6 to the resultsof the reaction conducted using an organic synthesis method of Morin etal., Organic and Biomolecular Chemistry, 10: 1517-20. PMID: 22246070(2012).

FIG. 15 is an illustration of the organic synthesis reaction ofmono-silylated dihydroxyacetone (DHA) used herein.

FIG. 16 is a drawing of chemical structures of GBLs used herein,contacted to cultures of microorganisms to determine effects onsecondary metabolite production. There are eight enantiomericstereoisomers of each of3-(1-hydroxyethyl)-4-(hydroxymethyl)dihydrothran-2(3H)-one and of3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one, forexample, see FIG. 10 .

FIG. 17 is a display of principal component analysis using Progenesis QIsoftware (Nonlinear Dynamics, Durham, N.C.). S. glaucescens wasfermented in SMM medium and was treated with GBLs3-(1-hydroxyethyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one (See, FIG. 16) and 3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one or acontrol untreated. LC-MS data of S. glaucescens fermentation culturestreated with GBLs3-(1-hydroxyethyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one and3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one and acontrol untreated S. glaucescens fermentation culture were analyzed. TheGBL treated S. glaucescens show concentration dependent deviations ofsecondary metabolites produced compared to controls in compoundsproduction. These results indicate induction of secondary metaboliteproduction resulting from S. glaucescens treatment with3-(1-hydroxyethyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one, in adose-dependent manner, and with3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one.

FIG. 18 are photographs of Escherichia coli confluent lawn in soft agarspotted with extracts of each of a S. coelicolor fermentation culturetreated with 3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one(See, FIG. 10 and FIG. 16 ), and a control untreated S. coelicolorfermentation culture. Extracts were fractionated on an HPLC column.Fractions of the treated extract, particularly fractions 28 and 41, showstrong bioactivity of3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one treated ininducing the production of the anti-bacterial activity S. coelicolorkilling E. coli bacteria as noted by circled zones. Strong antibacterialbioactivity resulted from induction of secondary metabolites bytreatment of S. coelicolor with 3-(1-hydroxyheptyl)-4(hydroxymethyl)dihydrofuran-2(3H)-one as seen compared to untreated S.coelicolor.

FIG. 19 is a photograph of a confluent lawn of Bacillus subtilis spottedwith fractions of either a S. coelicolor fermentation culture treatedwith 3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one or acontrol untreated S. coelicolor fermentation culture. Zones of clearing,shown in circles, indicate antibacterial activity of at least onecompound capable of killing B. subtilis. The results show appearance ofantibacterial activity capable of killing B. subtilis by S. coelicolorculture treated with3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one compared tountreated, particularly in fractions 28 and 41, shown in circles. Theseresults indicate induction of secondary metabolites in the treatedculture compared to untreated controls. A filter paper disk containing10 μg of Streptomycin was placed in the upper right and lower leftcorners of the lawn.

FIG. 20 is a mass chromatogram spectra of LC-MS data of fraction 28(FIGS. 18 and 19 ) of an extract of each of a 300 mL S. coelicolorculture grown in SMM and treated with GBL3-(1-hydroxyheptyl)-4-(hydroxymethyl) dihydrofuran-2(3H)-one and anuntreated control, respectively. The LC-MS data was obtained using aXevo G2-S Q-TOF mass spectrometer frpm Waters Corporation, Milford,Mass. The chromatogram trace with times of elution above the peaksindicates the treated fraction, and the trace below shows the controluntreated fraction. Peaks showing compounds induced by addition of GBL3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one wereobserved at retention times eluted at 1.48, 1.84, 1.99, 2.09 and 2.33.The peak at 1.84 was characterized as an unknown compound induced by S.coelicolor treatment with 3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one.

FIG. 21 is a mass chromatogram of the peak eluted at retention time 2.09from fraction 28 in FIG. 20 . The observed masses were determined tomatch those of iron-chelating compound Desferrioxamine E, see,Groenewold et al. “Collision-induced dissociation tandem massspectrometry of desferrioxamine siderophore complexes from electrosprayionization of UO₂ ²⁺, Fe³⁺ and Ca²⁺ solutions,” J Mass Spectrom 39: 7,752-761 (2004). The results show that Desferrioxamine E production wasinduced upon treating S. coelicolor culture with3-(1-hydroxyheptyl)-4-(hydroxymethyl) dihydrofuran-2(3H)-one.

FIG. 22 is a mass chromatogram of the peak eluted at retention time 1.81from fraction 28 in FIGS. 18, 19 and 20 . The observed masses weredetermined to match those of iron-chelating compound Desferrioxamine B,see, Groenewold et al., Ibid. The results show that Desferrioxamine Bproduction was induced by contact of S. coelicolor culture with3-(1-hydroxyheptyl)-4-(hydroxymethyl) dihydrofuran-2(3H)-one.

FIG. 23 is an mass chromatogram spectra of LC-MS data of fraction 41 asdescribed in FIGS. 18, 19 and 20 of the cultures treated with3-(1-hydroxyheptyl)-4-(hydroxymethyl) dihydrofuran-2(3H)-one and theuntreated control. The chromatogram trace with time points above thepeaks indicate the treated fraction, and the trace below shows thecontrol untreated fraction. Peaks showing compounds induced by additionof 3-(1-hydroxyheptyl)-4-(hydroxymethyl) dihydrofuran-2(3H)-one wereobserved at retention times 3.87 and 3.63.

FIG. 24 is a UV chromatogram of diode array HPLC detector analysis offraction 41 (FIGS. 18, 19, 20 and 23 ) of S. coelicolor cultures treatedrespectively with 3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one and untreated control. UV wavelength was set to272 nanometers. The peak observed to elute at retention time 3.83 in thetreated sample and not observed in the untreated control was determinedto be undecylprodigiosin, a known antibiotic with anti-cancer andimmunosuppressive properties. These results show that undecylprodigiosinproduction was induced by treatment of S. coelicolor with3-(1-hydroxyheptyl)-4-(hydroxymethyl) dihydrofuran-2(3H)-one.

FIG. 25 is a mass chromatogram of peak at retention time 3.8 as observedin FIG. 23 and FIG. 24 from fraction 41. The observed masses weredetermined to match those of the antibiotic undecylprodigiosin, see,Chen et al., “Unusual odd-electron fragments from even-electronprotonated prodiginine precursors using positive-ion electrospray massspectrometry,” Journal of the American Society for Mass Spectrometry,19: 12, 1856-1866 (2008). The results show that undecylprodigiosinproduction was induced by treating S. coelicolor culture with3-(1-hydroxyheptyl)-4-(hydroxymethyl) dihydrofuran-2(3H)-one.

FIG. 26 is a mass chromatogram of the peak eluted at retention time 3.6from fraction 41 in FIG. 23 . The observed masses were determined tomatch those of the antibiotic streptorubin B, see Chen et al., Ibid. Theresults show that streptotubin B production was induced upon treating S.coelicolor culture with 3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one.

DETAILED DESCRIPTION

Compositions and methods herein provide chemical tools that have thepotential to accelerate and increase antibiotic discovery faster thanever before. These compositions and methods are part of a strategy toreturn to natural product discovery as a source of new antibiotics. Thecompositions and methods provided herein are potential chemical keysnecessary to activate silent gene pathways. FIG. 2 shows activation inS. coelicolor of production of a purple antibiotic as a result ofspotting on the bacteria a solution of a racemic mixture ofnon-naturally occurring GBLs having formulas VIII and IX. This resultsin discovery of new antibiotics faster and more cost effectively thanusing previous techniques, and increases the likelihood of finding novelstructures.

An antibiotic biosynthesis operon is a group of genes that code for anantibiotic under similar or identical regulatory control. A challenge infinding new antibiotic leads is lack of keys to access the products ofsilent operons. There is an outstanding need for a technology platformto activate silent operons of microorganisms that potentially produceantibiotics. See, Lewis, Nature Reviews Drug Discovery 12: 371-387(2013). Genomic data show that current approaches access only a smallpercentage of available secondary metabolic genes because most organismsfail to produce antibiotics upon culture in the laboratory. Compositionsand methods herein replicate natural environment to activate silent genepathways in an organism. Small molecules that act as hormones thatdirectly control antibiotic production in Streptomyces are synthesized.Only 14 of these naturally occurring hormones have been isolated andclassified, the structures of which are shown in FIG. 4 .

Signaling hormones such as GBLs were discovered herein that activatesecondary metabolic pathways in strains of microorganisms to overexpressproduction, for compounds the expression of which were previously wereconsidered to be ‘silent’ or were underexpressed under laboratoryconditions, and compounds that previously have not been identified.Rather than attempting to use recombinant nucleic acid cloningtechniques isolate, engineer, and re-assemble potential secondarymetabolite producing gene clusters, the method herein activates existingpathways in vivo in microorganisms, which at present are underexpressedand are quiescent under physiological conditions absent the GBL.

Various embodiments of the invention herein provide a composition havingthe formula (VIII or IX):

in which R₁ is a hydroxyl, hydrogen, optionally substituted alkyl,halogen, cycloalkane, or —C(O)(R₃). Certain embodiments of thecomposition herein provide R₃ as a hydrogen, optionally substitutedalkyl, optionally substituted aryl, or halogen. Certain embodiments ofthe composition herein provide R₂ as a hydrogen, hydroxyl, optionallysubstituted alkyl, halogen, cycloalkane, or —C(O)(R₄). Certainembodiments of the composition herein provide R₄ as a substituted alkyl,or optionally substituted aryl, halogen, or cycloalkane.

For example, a composition is provided having formula VIII or IX inwhich R₁ is —OH and R₂ is methyl, ethyl, n-propyl, n-butyl, n-pentyl,n-hexyl, n-heptyl, or n-octyl. For example, further provided is acomposition having formula VIII or IX in which R₁ is —OH and R₂ isisopropyl, isobutyl, sec-butyl, tetra-butyl, isobutyl, sec-pentyl,isopentyl, iso-hexyl, 2-methylpentyl, 3-methylpentyl, 2,3-dimethylbutyl,2,2-dimethyl butyl, 2-methylhexyl, 3-methylhexyl, 2,2-dimethylpentyl,2,3-dimethylpentyl, 2,4-dimethylpentyl, 3,3,-dimethylpentyl,3-ethylpentyl, 2,2,4-trimethylbutyl, 2-methylpentyl, 3-methypentyl,4-methylpentyl, 3-ethylhexyl, 2,2-dimethylhexyl, 2,3-dimethylhexyl,2,4-dimethylhexyl, 2,5-dimethylhexyl, 3,3-dimethylhexyl,3,4-dimethylhexyl, 3-ethyl-2-methylpentyl, or 3-ethyl-3-methylpentyl.

Certain embodiments of the composition herein provide R₂ as anoptionally substituted alkyl chain having a length in a range selectedfrom the group of: one carbon to about eight carbons, one carbon toabout 12 carbons, and one carbon to about 20 carbons. In variousembodiments of the composition, the optionally substituted alkyl chaincontains at one or more positions in the chain a substituent selectedfrom the group consisting of: an alkyl, an aryl, an amino, a hydroxyl, acarbonyl, a halogen, or a sulfur group. Certain embodiments of thecomposition herein provide the optionally substituted aryl group as anaromatic group such as benzene, pyridine, thiazoles, and the like. Incertain embodiments, the optionally substituted aryl groups contain atone or more positions in the ring a substituent selected from thefollowing: alkyl, aryl, amino, hydroxyl, carbonyl, halogens, or sulfurgroups.

Various embodiments of the invention herein provide a composition forinducing or upregulating expression of genes involved in biosynthesis ofa bioactive microbial product by cells of a strain of a microorganism,the composition including: at least one synthetic non-naturallyoccurring derivative of a GBL, in a dose effective to increaseexpression of the genes and biosynthetic production of the product inthe cells. The term “synthetic non-naturally occurring” as used hereinis defined as a laboratory-produced organic synthesis product, which hasa chemical structure different from that of a known endogenouslyproduced GBL found in nature.

For example, the bioactive product has at least one activity selectedfrom the group of: anti-bacterial, anti-fungal, anti-viral,anti-helminthic, anti-spasmodic, anti-cancer, anti-malarial,anti-trypanosomal, complement inhibitory, immune stimulant,anti-inflammatory, immune suppressant, toxin neutralizing, diuretic, andherbicidal.

In certain embodiments of the compositions herein, the strain of themicroorganism is a mixture of a plurality of strains or species, and thecomposition is effective to upregulate expression of genes in at leastone of the strains or species. Certain embodiments of the compositionherein provide that the synthetic non-naturally occurring derivative ofthe GBL is chemically different from the GBLs listed in FIG. 5 ,including that the synthetic non-naturally occurring GBLs are differentfrom: S. griseus A-factor; S. viridochromogenes Factor I; S. lavendulaeIM-2; S. coelicolor SCB1, SCB2, and SCB3; anthracyclines from S.bikiensis and S. cyaneofuscatus and greater length hydrocarbon chains in2R3R and 2S3S; and S. virginiae butenolides VB-A, VB-B, VB-C, VB-D, andVB-E. The GBL in embodiments of the composition includes a coresubstituted at the 3 position by a substituent having the structuremethyl-R₁ and at the 2 position by a substituent having the structureselected from the group consisting of: ketone-R₂, alcohol-R₂,carbonyl-R₂, such that the substituent at the 2 and 3 position of theGBL are attached to the GBL core by recto (R) or levo (L) bonds, and R₁and R₂ are each independently selected from the group consisting of: alower alkane, an alkyne, an alkoxyl, an alkoxy, a halogen, a sulfide, anamine, a carbonyl, and an alkene selected from the group consisting of:an ethyl, an ethoxy, an ethoxyl, a propyl, a propoxy, a propoxyl, abutyl, a pentyl, a hexyl, a t-butyl, an s-butyl, an i-butyl, ani-pentyl, an i-hexyl, and an i-heptyl.

Certain embodiments of the compositions have the GBL core substituted atthe 2 or 3 position with a lower alkane having a length of one carbon toabout eight carbons. Alternatively, in embodiments of the composition,the GBL core is substituted at the 2 or 3 position with an alkane havinga length greater than eight carbons. For example, embodiments of thecomposition provide GBLs that have a chemical structural formula fromthe group consisting of molecules having the formulas I-VII in FIG. 10 .Certain embodiments of the compositions here provide that the R₁ is ahydroxyl and is either recto-(R) or levo-(L), and R₂ is a hexylsubstituent which is R or L.

An embodiment of the invention herein provides a method of improving ayield of a microbially-produced bioactive secondary metabolite product,the method including contacting cells of a strain of microorganism witha suitable amount of at least one GBL composition in which the GBL isnon-cognate to the strain or is synthetic and non-naturally occurring,and culturing the cells of the strain with the GBL under conditions forproduction of the product; and, obtaining the product from the cellfermentation culture by separation of cells and medium or purificationof the product from the cells and analyzing the amount of the product,such that the yield of the product per unit of volume of culture orweight of cells is greater than that from control cells of the strainnot contacted with the GBL composition and otherwise identicallycultured and analyzed, such that the yield of the product from the cellscultured with the derivative of the GBL is improved compared to thatfrom the control cells.

The strain of the microorganism is generally bacterial, fungal, oralgal. For example, the strain of microorganism is bacterial and is anactinomycete. For example, the actinomycete is a genus selected from thegroup of genera consisting of: Actinopolyspora, Amycolatopsis,Micromonospora Nocardia, Pseudonocardia, Saccharothrix,Saccharopolyspora, Salinospora, Streptomyces, Tetinomedara, andVerrucosispora. In a further example, the actinomycete is at least onestreptomycete selected from the group of: Streptomyces avermitilis, S.aureofaciens, S. capreolus, S. cattleya, S. clavuligerus, S. coelicolor,S. fradiae, S. garyphallus, S. griseus, S. kanamyceticus, S. levoris, S.lincolnensis, S. niveus, S. noursei, S. platensis, S. plicatus, S.pristinaespiralis, S. orientalis, S. ribosidifus, S. rimosus, S.roseosporus, S. scabiei, S. venezuelae, S. vinaceus, and S. virginiae;or is at least one Pseudonocardia selected from the group of: P. acacia;P. ailaonensis; P. adelaidensis; P. alaniniphila; P. ammonioxydans; P.carboxydivorans; P. halophobia; P. kujensis; P. nitrificans; P.petroleophila; P. salamisensis; P. sulfoxidans; P. thermophila; and P.zigingensis; or is at least one Amycolatopsis selected from the groupof: A. alba, A. azurea, S. balhimycena, A. coloradensis, A. fastidiosa,A. keratiniphila, A. lurida, A. mediterranei, A. orientalis, A.sulphurea, A. tolypomycina, and A. vancoresmycina.

An embodiment of the method includes a derivative of the GBL that issynthetic and non-naturally occurring and is at least one of thecompositions selected from formulas I-VII in FIG. 10 . Embodiments ofthe method result in the yield from the cells contacted with the GBLhaving at least about two-fold great, four-fold great, ten-fold greater,twenty-fold, fifty-fold, or hundred-fold greater than the yield from thecontrol cells.

Embodiments of the invention herein provide a method of discovery of acell-produced secondary metabolic compound in a microbial straincontaining putative unexpressed or under expressed genes encodingenzymes for biosynthesis of a chemical entity having a medicinal orindustrial biological activity, the method including: contacting atleast one cell sample or a plurality of cell samples, the samplescontaining mixtures of cells from a plurality of microbial strains witha suitable amount of at least one synthetic GBL in which the microbialstrains are selected from the group of: fresh isolates from nature,naturally occurring mixtures of unpurified microorganisms, and anestablished species strain such that the GBL and the established speciesare non-cognate; culturing the cell samples with the GBL derivativeunder conditions for production of secondary metabolite chemicalcompounds; screening the cultures by at least one detection system forpresence of the biological activity, such that the presence of theactivity identifies the producing sample containing at least one strainof microorganism producing the chemical having the activity; and,characterizing at least one chemical structure having the biologicalactivity, and comparing the structure to a library database of knownchemical entities to obtain chemicals not previously known, therebyscreening to discover the chemical compounds with the biologicalactivity.

“Synthetic” as used herein is defined as a laboratory-produced organicsynthesis product, which has a chemical structure that either isnaturally occurring or non-naturally occurring. “Non-cognate” as usedherein is defined as a signaling molecule, such as a GBL, that isexogenously supplied to the microorganism and is not known at the timeof the current application to be endogenously produced by thatmicroorganism, or at the time that microorganism is screened in thepresence of the signaling molecule using the methods herein.“Non-naturally occurring” a used herein is defined as having a chemicalformula and/or a steric configuration not know to be produced by anorganism found in nature.

1. Certain embodiments of the method herein provide that the methodfurther include, prior to screening, mixing cells to obtain the samplesof the plurality, such that each sample of the at least one or theplurality contains at least two, at least five, or at least 10 strains.Certain embodiments of the method provided herein, the GBL is aplurality of GBLs each having a different chemical structure. Forexample, at least one or the plurality includes at least one, at leasttwo, at least four, at least five, or at least ten GBLs, each having adifferent chemical structure. The different chemical structure includesGBLs that are racemates or a racemic mixture, and racemates includethose that are non-naturally occurring. In embodiments of the methodherein, the screening further includes contacting each of the samples tothe detection system which is an assay including at least one componentselected from the group of: an organism, a tissue, a cell culture, andan enzyme of a detection system; and measuring an activity selectedfrom: anti-bacterial, anti-fungal, anti-viral, anti-helminthic,anti-cancer, anti-malarial, anti-trypanosomal, complement inhibitory,immune stimulant, anti-inflammatory, immune suppressant, toxinneutralizing, diuretic, and herbicidal.

In embodiments of the culturing step, growing the cells of the strain ofmicroorganism identified as producing the chemical is performed in aliquid medium, and the method further includes prior to screening,separating the cells from the medium to obtain a resulting supernatantdepleted of the cells. Alternatively, culturing is growing the cells ofthe strain of microorganism in contact with soil. In embodiments of themethod herein, the method further includes prior to screening,separating the cells from the soil and washing the soil and cells, toobtain a resulting supernatant enriched for extracellular products.

An embodiment of the method herein provides after identifying, isolatingthe chemical compound from the producing culture contacted with the GBL.The method further may include isolating the at least one GBL from theplurality of GBLs contacted to the sample that induces expression of theproduct. The method provides characterizing the chemical structure andanalyzing by at least one method selected from the group consisting of:mass spectrometry (MS), gas chromatography, thin layer chromatography,matrix-assisted laser desorption/ionization (MALDI), MALDI-time offlight (MALDI-TOF), moving bed chromatography, and high performanceliquid chromatography (HPLC). Embodiments of the method herein provideculturing alternatively, as growth of the strain or strains on solidmedium. Using solid medium, screening further includes adding cells of atarget indicator strain including at least one of a bacterium, a fungus,a eukaryotic cell, a white blood cell, and a eukaryotic tissue explant.The method further includes testing a sample of the supernatant from aliquid culture in a test subject which is an experimental animal modelof a disease. The method alternatively provides a further step oftesting a sample of the supernatant in vivo in cultured cells or tissuesof a mammal, a plant, or an insect.

Embodiments of the method herein provide a further step of obtainingcoordinates of peaks observed by MS, MALDI, MALDI-TOF, or HPLCcorresponding to presence of the secondary metabolism products of thestrain of the microorganism, and comparing the location of the peaks tothat of known previously. characterized products to identify novelchemical entities. Certain embodiments of the method herein provide astep of screening separately each of the plurality component strains forproduction of the novel chemical entities, to identify which strainproduces the novel entity. Such a method was used herein to obtaininduction of synthesis of a potentially novel compound from a culture ofS. coelicolor having characteristics different from those in a databaselibrary, and eluting in a peak at 1.84 by liquid chromatography.

Various embodiments of the invention herein provide a method ofincreasing or accelerating production of a microbial secondarymetabolism compound, the method including: contacting a culture of aproducing microorganism strain with a GBL at an effective dose toupregulate expression of genes encoding enzymes that synthesize thecompound, in which the GBL is non-cognate to the strain. The non-cognateGBL is, for example, synthetic and non-naturally occurring, or is notnative and not endogenously made by the producing microorganism strain.

In alternative embodiments of the method herein, the GBL is added at orbefore inoculation of production culture medium with the microorganism;or the GBL is added after inoculation, or during growth of the cells ofthe strain; or the GBL is added at stationary phase or after cessationof growth of the cells of the strain; or the GBL is added at a pluralityof time points during culture of the micro-organism.

Various embodiments of the invention herein provide a method of organicsynthesis of a GBL having a formula of:

the method including: acylating 2,2-dimethyl-1,3-dioxane-4,6-dione(Meldrum's acid) in a mixture of a pyridine and anhydrousdichloromethane (CH₂Cl₂), and esterifying the acylated2,2-dimethyl-1,3-dioxane-4,6-dione with a mono-TBDMS(tert-butyldimethylsilyl) protected dihydroxyacetone to form abeta-keto-ester and mixing with toluene and heating a resulting mixture;condensing the heated mixture of the beta-keto-ester and the toluenewith an excess of silica under conditions in which a Knoevenegalcondensation results in a protected butenolide bound to the silica atroom temperature and purifying by further silica using a column to elutethe protected butenolide; and reducing the butenolide with sodiumcyanoborohydride to form a 2,3 di-substituted gamma-butyrolactone, anddeprotecting the 2,3 di-substituted GBL at room temperature to form theGBL having the formula of VIII or IX.

In various embodiments of the method, R₁ is provided as at least onemoiety selected from the group consisting of a hydroxyl, a hydrogen, anoptionally substituted alkyl, a halogen, a cycloalkane, and a —C(O)(R₃).Further, R₃ is at least one selected from the group of a hydrogen, anoptionally substituted alkyl, an optionally substituted aryl, and ahalogen. Further, R₂ is at least one selected from a hydrogen, ahydroxyl, an optionally substituted alkyl, a halogen, a cycloalkane, anda —C(O)(R₄). R₄ is at least one selected from the group consisting of: asubstituted alkyl, an optionally substituted aryl, a halogen, and acycloalkane. For example, the optionally substituted alkyl chaincontains at least 8 carbon atoms, at least 12 carbon atoms, or at least20 carbon atoms. For example, the optionally substituted alkyl issubstituted at one or more carbons in the chain with at least onesubstituent selected from an alkyl, an aryl, an amino, a hydroxyl, acarbonyl, a halogens, and a sulfur group. For example, the optionallysubstituted aryl is an aromatic moiety selected from the groupconsisting of: benzene, pyridine, and thiazoles. For example, theoptionally substituted aryl is substituted at one or more positions inthe ring with at least one substituent selected from the groupconsisting of: an alkyl, an aryl, an amino, a hydroxyl, a carbonyl, ahalogen, and a sulfur. Various embodiments of the invention hereinprovide a method of organic synthesis of a GBL including acylating2,2-dimethyl-1,3-dioxane-4,6-dione (Meldrum's acid) in a mixture of apyridine and anhydrous dichloromethane (CH₂C₁₂); esterifying theacylated 2,2-dimethyl-1,3-dioxane-4,6-dione with a mono-TBDMS(tert-butyldimethylsilyl) protected dihydroxyacetone to form abeta-keto-ester; and reducing the butenolide with sodiumcyanoborohydride to form a 2,3 di-substituted GBL; and deprotecting the2,3 di-substituted GBL at room temperature to form with an improvementincluding, prior to deprotecting:

mixing the beta-keto-ester with toluene and heating a resulting mixtureon silica; and condensing the heated mixture of the beta-keto-ester andthe toluene with silica, prior to purifying, under conditions in which aKnoevenegal condensation results in a protected butenolide bound to thesilica at room temperature, resulting in obtaining an improved yield anda quicker reaction. For example, the reaction yields a butenolide inabout two to three hours.

Certain embodiments of the method herein provide the step of, prior toesterifying acylated Meldrum's acid, combining dichloromethane and acatalyst that is 1-methylimidazole to form mono-TBDMS(tert-butyldimethylsilyl) protected dihydroxyacetone.

Example 1 Acylation of Meldrum's Acid as a Step of Organic Synthesis ofGBLs

Hormones that are novel because they are not found in nature aresynthesized using organic chemistry methods herein. The non-naturallyoccurring hormones were contacted to cells of Streptomyces species todetermine antibiotic production, as visualized by the induction of thepigmented antibiotic actinorhodin or some other detection assay. Thehormones synthesized and analyzed herein were not native to S.coelicolor, viz., the hormones are not endogenously produced and henceare non-cognate with respect to this species. GBL signaling moleculesused herein include, but are not limited to, VB-C, VB-D, and A-Factor.

The organic synthesis of a GBL is shown in FIG. 6 . Meldrum's acid wasacylated with acyl-halides yielding a diverse number of analogues. Toacylate Meldrum's acid, a 250 mL round bottom flask was charged with17.76 g (0.123 mol) recrystallized Meldrum's acid(2,2-dimethyl-1,3-dioxane-4,6-dione). A stir bar and 65 mL anhydrousdichloromethane was added to the flask. The flask and its contents werecooled in an ice bath. Anhydrous pyridine, 24.3 mL (0.30 mol), was addeddropwise to the Meldrum's acid over a 10 minute period. Meldrum's acidwas combined with other reagents in parts because the acid decomposes atthe higher temperatures. Heptanoyl chloride, 19.04 mL (18.27 g/0.123mol), was added drop-wise over a 2 hour period to the clear solution in50 mL anhydrous dichloromethane. After the 2 hour addition period, thereaction was stirred on ice for 1 hour, then brought to room temperatureand stirred for an additional 1 hour. Yields of acylated Meldrum's acidwere surprisingly greater than 90% using heptanoyl chloride in DCM driedover NaSO₄, and without the use of a nitrogen atmosphere. See, OrganicSyntheses, Coll. Vol. 7, p.359 (1990); Vol. 63, p.198 (1985).

The reaction mixture was diluted with an additional 50 mLdichloromethane, then washed twice with 50 mL partitions of 2N HCl. Theaqueous phase was extracted three times with dichlormethane, and theorganic phases pooled, washed once with saturated NaCl, and dried overanhydrous sodium sulfate. Dichlormethane was removed with rotaryevaporation to yield a pale yellow/deep red/orange oil or solid as aproduct.

Example 2 Alternative Synthesis Procedures for Acylation of Meldrum'sAcid

Recrystallized Meldrum's acid is added to a round bottom flask of anappropriate size. An organic solvent such as hexane, dichlormethane,chloroform, heptane, toluene, dichloroethane, or cyclohexane, was addedto the flask. The flask and its contents are cooled in an ice bath. A2.5 mol equivalent of anhydrous pyridine was added dropwise to theMeldrum's acid over a period of time of either 5 seconds, 30 seconds, 5minutes, 10 minutes, 30 minutes, 60 minutes, or 24 hours. A solution ofan acyl-halide at a molar ratio of 0.005, 0.010, 0.150, 1, 2, 3, 5, or10 was added to the clear solution of Meldrum's acid and catalyst over aperiod of 5 seconds, 30 seconds, 5 minutes, 10 minutes, 30 minutes, 1hour, 2 hours, 5 hours, 10 hours, or 24 hours.

Example 3 Deprotection and Esterification Techniques to Provide ImprovedReaction Time and Yield

Reactions forming mono-silylated dihydroxyacetone (DHA) are shown inFIG. 15 . The protection reaction shown at the top of the figure usingimidazole and DMF yields di-protected, mono-protected, and thetert-butyldimethylsilyl ether (TBDMS). DMF removal is challenging usingthis method, and the deprotecting reaction runs overnight. Methodsprovided herein were devised to replace the catalyst imidazole with1-methylimidazole, and the results reduced reaction time from 17 hoursto 15-20 minutes. The recovery for reactions using 1-methylimidazole asa catalyst was about 50%.

Esterification of the crude reaction containing TBDMS-DHA and acylatedMeldrum's acid yielded a crude reaction of uncyclized ester andbutenolide. Mono-protected DHA species protected with a TBDMS group wasreacted with acylated Meldrum's acid species to yield beta-keto-ester.Immediately following consumption of mono-DHA, the reaction was stoppedand combined with 110° C. toluene. While still hot, the mixture waspoured over a small amount of silica in a beaker (1 g crude reaction to2 g silica) to form β-keto-ester. This mixture was reacted for one hourand then stored at −20° C. overnight.

Beta-keto-ester was formed as hot reaction mixture was heated on amixture of silica for about an hour to improve the cyclization of theester into the butenolide. Beta-keto-ester was cyclized into substitutedbutenolide in about 10-15 minutes. Alternatively, it is envisioned thatdimethylformamide and imidazole are substituted in place ofdichlormethane and 1-methylimidazole. After butenolide formation, themixture was loaded onto a silica column for purification.

In an alternative method, the crude reaction is loaded directly onto acolumn containing four times excess of silica for purification, and thecolumn is incubated and sits overnight. See, Morin et al., Organic andBiomolecular Chemistry, 10: 1517-20. PMID: 22246070 (2012).

The photographs of TLC results in FIG. 14A-14C show the completedisappearance of the purple ester and full formation of blue butenolide,which indicates an improved yield for the synthesis method used herein.

The traditional method of butenolide formation is a “spontaneous”reaction with a low yield as evidenced by the purple spots at the bottomof the chromatogram in FIG. 14A. The chromatogram of FIG. 14B comparisonof the traditional method yield with the modification indicates that thetraditional method results in a high volume of products and a low yieldof butenolide.

Greater energy was entered into the reaction performed herein by furtherheating the reaction mixture prior to combining with silica, which mayhave improved efficiency in the presence of the Lewis Acid catalyst (thesilica gel), as shown the presence of blue spots and fewer purple spotsin FIG. 14B. Allowing the mixture to remain on silica overnight wasobserved to result in nearly complete cyclization of ester into abutenolide as shown by an increase in blue spots and lack of purplespots in FIG. 14C.

After the butenolide was formed, reduction was necessary to yield theGBL. Sodium cyanoborohydride in ethanol was used, which reduced thebutenolide within 30 minutes. Because excessive reduction may occur atthe ketone yielding an alcohol, the reaction was monitored and quenched.Excessive reduction provides access to the VB type and IM type GBLs.After reduction, deprotection was performed to yield a racemic mixtureof 2, 3-disubstituted GBL species having formulas VIII and IX. It isenvisioned that the non-naturally occurring GBLs may have at least oneof the function group modifications in FIG. 11. For example, analogs ofA-factor type, VB type, and SCB type of GBLs that can be synthesized andtested for activity to induce antibiotic production, as shown in FIG. 13.

Example 4 Use of a Racemic Mixture of GBLs to Screen for AntibioticProduction

The formulas I-VII in FIG. 10 illustrate the structures of theenantiomers in the mixture of GBLs tested for ability to elicitantibiotic production, the results of which are shown in the plates inFIG. 9 . Each GBL has the same gross chemical formula with differentchirality at asymmetric carbons, hence have different three-dimensionalstructures and are enantiomers. The mixture of GBLs was added to a pureculture of non-cognate microorganism S. coelicolor. Streptomycetestrains were cultured in complex medium R5 or in minimal medium MMS. SeeKieser, T. et al., Practical Streptomyces Genetics, John InnesInstitute, 2000. Data obtained show that production of an antibacterialactivity was elicited, which are the dark circles (pigmented secondarymetabolites) produced on solid medium and which was found to be producedas a function of the amount of the GBLs deposited per plate. Racemicmixtures of enantiomers were contemplated to be more efficient from atesting standpoint because multiple biologically active GBLs could betested in a single assay, so that the assay is a multiplex test of theeight enantiomers. VB-D is a naturally occurring GBL of S. virginiae,and is non-cognate to S. coelicolor, which was used as a test strain ofmicroorganism to determine effect on antibiotic production. This speciesis known to produce a purple antibiotic, actinorhodin, production ofwhich is used as a model system for studies of regulation of antibioticbiosynthesis. The dark areas in the plates in FIG. 9 results fromproduction of the purple antibiotic actinorhodin.

Spore stock of S. coelicolor was used to inoculate SMMS agar (solid SMMmedium) and the spore suspension on the surfaces of the plates wasallowed to dry. The GBL amounts were added at the time of inoculation.No antibiotic production was observed on the plates after 24 only hours.

The two plates in the top of the photograph of FIG. 9 are controlscultures of S. coelicolor. The control plate on the left is a negativecontrol in which no GBL nor vehicle was added. The control plate on theright was contacted with the vehicle only, which was a mixture ofmethanol and water.

A racemic mixture of GBLs containing the non-naturally occurringcompounds I-VII and virginiae butenolide-D (VB-D) was synthesized, andan amount of about 500 μg was dissolved in 100 μL of vehicle to yield a5 mg/ml concentration solution. The plates of the second row from leftto right were spotted with 20 μL (100 μg), 10 μL (50 μg), 5 μL (25 μg),and 1 μL (5 μg) of the 10 mg/ml concentration solution, respectively.The first four plates from left to right of the third row were spottedwith 20 μL (50 μg), 10 μL (25 μg), 5 μL (12.5 μg), and 1 μL (2.5 μg) ofa 1:2 dilution of the 10 mg/ml concentration solution which had a 2.5mg/mL concentration, respectively. The fifth plate of the third row wasspotted with 2 μL (1 μg) of a 1:10 dilution of the 10 mg/mlconcentration solution. It was observed after 42 hours that each of theexperimental plates produced antibiotic evidenced by the dark spot andthe production was dose-dependent monotonically on amount of GBL.

Example 5 Bacterial Culture

Streptomyces species used in methods herein were altered and testedusing the methods provided in Hopwood et al., Genetic Manipulation ofStreptomyces a Laboratory Manual (1985), which is hereby incorporated byreference in its entirety. Further, this reference provides culturetechniques, media preparation, temperature and additional cultureconditions, recombinant production and manipulation of Streptomycesspecies. Additional media are described in Kieser, T. et al., Ibid.Special culture conditions of media and temperature for spore productionin various strains are well-known in the art and are indicated byspecies for bacteria in Bergey's Manual of Systematic Bacteriology, Vol.1-5 (2001-2012), New York, N.Y., Springer-Verlag. See also, DifcoManual, 2^(nd) Ed. 1009, B-D, Sparks, Md.

Microorganisms were contacted or treated with natural, cognate,non-cognate, and synthetic non-signaling hormones that activate and/oroverexpress gene clusters responsible for secondary metabolite synthesisin the cells. Methods are provided herein for discovery and design ofGBL-like compounds that improve yields of antibiotics produced bymicroorganisms. For example, the microorganism is a strain of bacteria,fungi, protozoa, viruses, or microalgae, which is a non-limiting list.Previously unknown bioactive compounds from known and unknownmicroorganism strains of species are discovered by methods herein.Environments are sampled to screen for producing strains, theenvironments including but not limited to, fresh water sediment,seawater sediment, soils such as from forest, farmland, tundra, alpineregion, or landfill. Special media may include sterile or freshenvironmental components. See, Lewis K. et al., Nature Reviews DrugDiscovery 12: 371-387 (2013).

Example 6

Non-Cognate GBL Induction of Antibiotic Biosynthesis in S. coelicolor byNon-Naturally Occurring Synthetic GBLs

Two non-naturally occurring GBLs designed and synthesized by the methodsherein have a formula of X and XI, respectively, and are shown in FIG. 8. These GBLs were analyzed for ability to increase antibiotic productionin S. coelicolor.

Results with treated plate cultures and untreated plate controls nottreated with GBLs are shown in FIGS. 3 and 7 , in which pigmentedantibiotic is produced only in response to treatment by the non-cognatesynthetic non-naturally occurring GBL. FIGS. 3 and 7 are photographs ofS. coelicolor in which positive antibiotic production was obtained as aresult of increased amount of GBL applied to the respective plate.

FIG. 12 is a photograph of SMMS (supplemented minimal media solid)plates inoculated with a spore stock of S. coelicolor streaked to coverthe surface of the medium in the plate. At the time of inoculation, 2 μLof a racemic solution containing each amount of a dilution of theracemic GBLs having formulas X and XI were deposited in the center of aplate. Plate 1 a was spotted with 2 μL of a solution containing 16.5 μgof GBLs X and XI. Plates 2a and 2b were spotted with 2 μL of a solutioncontaining 33 μg of GBLs X and XI. Plate 3a was spotted with a solutioncontaining 49.5 μg of GBLs X and XI. Plates 4a and 4b were spotted witha solution containing 66 μg of GBLs X and XI. Plates 5a, 6a, 7a, werespotted with solutions containing 99 μg, 132 μg, and 165 μg of GBLs Xand XI, respectively. Racemic mixture GBLs were present in equal molaramounts. The plates spotted with 16.5 μg, 33 μg, 49.5 μg, 66 μg, 99 μg,132 μg, or 165 μg amounts of GBLs having formulas X and XI were observedto have increased production of pigmented antibiotics known to beproduced by the strain S. coelicolor for which these GBLs arenon-cognate. No pigment production was observed on the control platesshown in FIG. 7 not contacted with GBLs. Further, contacting the plateswith GBLs was observed to result also in early induction of productionof the pigmented antibiotics.

Example 7

Principal Component Analysis of S. glaucescens Cultured under 96Conditions of Media and GBL Supplementation

S. glaucescens cells were grown in 3 mL cultures under 96 differentconditions of medium, GBL choice, and GBL concentration. Each GBLsolution was added to a tube in each of the following concentrations:0.2 μM, 0.8 μM, 4 μM., 20 μM, and 100 μM. Media were a minimal mediumSMM or a yeast enriched complex medium R5 (also called R2YE). The GBLindicated in FIG. 17 as PR001 and PR002 are shown in FIG. 16 , and havethe chemical formulae, respectively:

-   -   3-(1-hydroxyethyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one; and,    -   3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one.

Fermentations were incubated in 24-well blocks (CR 424, Enzyscreen B.V.,Netherlands) with lids (1221a), and were shaken at 200 rpm for 5 days at28° C. in an Infors HT incubator (Infors AG, Switzerland). For analysis,a C18 SPE-IT tip (57234-U from Sigma-Aldrich) was added to eachfermentation which were further shaken at 400 rpm for one hour. Tipswere removed and rinsed in deionized water, and were analyzed directlyor stored for analysis. Analysis was collected at ionsense, Inc.(Saugus, Mass.) vaporized with a DART source at 400 C and 1 mm/s, andmass spectral data collected in a Thermo LTQ. Analysis used ProgenesisQI from Nonlinear Dynamics (Waters).

Principal component analysis data of secondary metabolites induced bythe GBLs in comparison to control absent GBL are shown in FIG. 17 . Thetwo principal component concentrations of components 1 and 2 aredisplayed on ordinate and abscissa. The data revealed that greatestdistinction from control secondary metabolites produced absent GBL wasobtained by addition of3-(1-hydroxyethyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one. Further,this induction was dose dependent, with maximal distinction obtained at100 μM, and lesser distinction at each lower concentration. Accordingly,100 μM GBL was used in large scale fermentions.

The initial large scale fermentation below was performed with S.coelicolor since this is a very well characterized species known toproduce multiple antibiotics, to determine whether a syntheticnon-cognate GBL, VB-D, and seven non-naturally occurring enantiomers,induce greater production of antibiotics and induce otherwise silentgene clusters to produce novel antibiotics.

Example 8

Identifying Novel Chemical Entities from Crude Extracts

Yields of both known and unknown bioactive compounds regulated by thepresence of signaling hormones are improved by contacting producingcells with an appropriate GBL. Secondary metabolites were isolated fromcultures of cells. Triplicate 300 mL cultures of S. coelicolor in SMM,was treated with the synthetic racemic mixture of VB-D and sevenenantiomers of the non-cognate GBL shown in FIG. 10 , at a totalconcentration of 100 μM, and an identical culture was grown without GBL.Cells were grown for five days at 29 C shaking at 220 rpm. Triplicateswere pooled with GBL-treated and control cultures pooled separately.

A slurry of absorbent resins HP-20, XAD-16, XAD-7 and XAD-4 was added(2-4% weight/volume) and shaking was continued overnight. The resin andcell mass were removed by filtration and were washed three times with200 mL deionized water. Resin and cell mass were extracted three timeswith 100-300 mL methanol to elute secondary metabolites from the resin.This extract was concentrated by rotary evaporation to remove extractionsolvent.

The crude extract was dissolved in 1-3 mL of dimethylsulfoxide (DMSO)and was injected into a reveleris C18 reverse phase column on a GilsonHigh-Pressure Liquid Chromatography system. A flow rate of 15 ml/min wasrun for 40 minutes using mobile phases of methanol with 0.1% formicacid, and water with 0.1% formic acid. Forty-eight fractions werecollected from a twenty minutes gradient of solvent from 15% methanol to95% methanol, and were analyzed for antibacterial content on soft agarlawns of each of a Gram negative indicator strain, Escherichia coli, anda Gram positive indicator strain, Bacillus subtilis.

Further, 10 μL fraction volumes of each fraction were injected into aWaters Xevo G2-S Q-TOF LCMS system for further analytical separation andmass identification. Results are shown in Examples below.

Example 9 Bioassays of Fractions of Extracts

Fractions 1-48 of each of fractionated extracts of the GBL-treated anduntreated control fermentations were assayed for antibacterial activityto obtain fractions showing activity as a result of the contact with theGBL. Results are shown in 17 and 18.

Control fractions data are shown in the top plate and GBL-treatedfraction data shown in the bottom plate of FIG. 18 , which are zones ofkilling of Gram negative E. coli cells. These plates start with fraction25 assayed at the top left, and extend through fraction 48 at the bottomright of each plate. The results observed in these assays clearly showthat fractions 28 and 41 of the GBL-treated extract contain at least onecompound with antibacterial activity, and the corresponding fractions inthe control extract does not.

Data in FIG. 19 with cells of Gram positive bacteria, B. subilis, areeven more dramatic. Fractions 28 and 41 contain strong antibacterialactivity in GBL-treated extracts, and the corresponding fractions fromcontrol extract failed to kill cells.

Accordingly, these fractions were analyzed by chemical techniques tofurther characterize the contents.

Example 10 Mass Spectroscopic Analysis of Antibacterial FractionsInduced by GBLS: Fraction 28

Fraction 28 of each of the GBL and the control extracts were eachanalyzed by LC-MS-TOF. Data obtained with fraction 28 treated andcontrols superimposed are shown in FIG. 20 . The trace for GBL-treatedextract showed a greater total amount of material, and containedcompounds with peaks eluting at time points 1.48, 1.84, 1.99, 2.09, and2.33 which were not observed in the control extract.

The peak at retention time 2.09 was further analyzed by masschromatogram, and it was observed that the parent masses and thefragmentation masses match that of the iron-chelating siderophoreDesferrioxamine E the structure of which is shown in the figure abovethe data, as parent ion calculated mass 601.35 was observed. Daughterions match that of published data.

The peak at retention time 1.81 was further analyzed by masschromatogram, and it was observed that the parent masses and thefragmentation masses match that of the iron-chelating siderophoreDesferrioxamine B the structure of which is shown in the figure abovethe data, as parent ion calculated mass is 560.34 and the observed massis 561.26. Daughter ions match that of published data.

These data show that production of both Desferrioxamine B andDesferrioxamine E was substantially enhanced or even induced by thesynthetic non-cognate GBL.

Example 11 Mass Spectroscopic Analysis of Antibacterial FractionsInduced by GBLS: Fraction 41 and an Unknown Chemical Entity

Fraction 41 of each of the GBL and the control extracts were eachanalyzed by LC-MS-TOF. Data obtained with fraction 41 treated andcontrols superimposed are shown in FIG. 23 . The trace for GBL-treatedextract showed a greater total amount of material, and containedcompounds with peaks eluting at time points 1.80, 3.63, and 3.87 whichwere not observed in the control extract. Fraction 41 was subjected toUV chromatogram of diode array HPLC detector analysis. Again atprominent peak at 3.83 was observed. This material was determined to beundecylprodigiosin by mass chromatogram shown in FIG. 25 , which has anobserved mass of 393.27 and a calculated mass of 394.25. These data showthat production of undecylprodigiosin was substantially enhanced or eveninduced by the synthetic non-cognate GBL.

The peak in fraction 41 of 3.62 was determined to be Streptorubin B asshown in FIG. 26 . This known antibiotic has a claulated mass of 391.26and the mass observed here was 392.23. These data show that productionof Streptorubin B was substantially enhanced or even induced by thesynthetic non-cognate GBL.

The 1.84 peak of fraction 28 seen in FIG. 20 was analyzed, and is apotential novel chemical entity, as the data obtained do not correspondto literature reports.

Other microorganisms were subject to the small scale fermentations andprincipal component analyses to determine optimal GBL indentificationand concentrations, and to large scale fermentations as in the examplesherein and the extracts obtained were subject to the chromatographicanalyses performed above. Strains were chosen from Table 1 below, whichis a list of suitable wild type or commercially interesting species, forsmall and large scale fermentations and extract analyses.

Embodiments of the method and composition having been fully describedherein are further exemplified in the claims, which are not to beconstrued as further limiting. The contents of all references citedherein are hereby incorporated by reference in their entireties.

What is claimed is:
 1. A composition for upregulating biosynthesis andproduction of a bioactive microbial product by cells of a sample ofmicroorganisms, the composition comprising: at least one syntheticnon-naturally occurring derivative of a γ-butyrolactone (GBL) core, in adose effective to increase expression of the genes and biosyntheticproduction of the product in the cells.
 2. The composition according toclaim 1, wherein the bioactive product has at least one activityselected from the group consisting of: anti-bacterial, anti-fungal,anti-viral, anti-helminthic, anti-cancer, anti-malarial,anti-trypanosomal, complement inhibitory, toxin neutralizing, immunestimulant, anti-inflammatory, immune suppressant, diuretic, andherbicidal.
 3. The composition according to claim 1, wherein the sampleof the microorganism is a mixture of a plurality of strains or species,and the composition is effective to upregulate expression of genes in atleast one of the strains or species.
 4. The composition according toclaim 1, wherein the synthetic non-naturally occurring derivative of theGBL has a chemical structure different from naturally occurring GBLs oris a non-naturally occurring stereoisomer of a GBL, and the compositionstructure is not the same as: Streptomyces griseus A-factor; S.viridochromogenes Factor I; S. lavendulae IM-2; S. coelicolor SCB1,SCB2, and SCB3; anthracyclines from S.bikiensis; S. cyaneofuscatusgreater length hydrocarbon chains in 2R3R and 2S3S; and S.virginiaebutanolides VB-A, VB-B, VB-C, VB-D, and VB-E.
 5. The compositionaccording to claim 1, wherein the GBL comprises a core which issubstituted at the 3 position by a group having the structure methyl-R₁and at the 2 position by a group having the structure selected fromketone-R₂, alcohol-R₂, and carbonyl-R₂, wherein the substituent at the 2and 3 position of the GBL are attached to the GBL core by recto (R) orlevo (L) bonds, wherein R₁ and R₂ are each independently selected fromthe group consisting of: a lower alkane, an alkyne, an alkoxyl, analkoxy, a halogen, a sulfide, an amine, a carbonyl, and an alkeneselected from the group consisting of: an ethyl, an ethoxy, an ethoxyl,a propyl, a propoxy, a propoxyl, a butyl, a pentyl, a hexyl, a t-butyl,an s-butyl, an i-butyl, an i-pentyl, an i-hexyl, and an i-heptyl.
 6. Thecomposition according to claim 5, wherein the GBL core is substituted atthe 2 or 3 position with a lower alkane having a length of 1 carbon toabout 8 carbons.
 7. The composition according to claim 5, wherein theGBL core is substituted at the 2 or 3 position with an alkane having alength greater than 8 carbons.
 8. The composition according to claim 5,wherein the R₁ comprises hydroxyl and is either recto-(R) or levo-(L),and R₂ comprises a hexyl which is R or L.
 9. The composition accordingto claim 1, selected from at least one enantiomer or stereoisomer of thegroup consisting of 3-(1-hydroxyethyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one; 3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one;3-acetyl-4-(hydroxymethyl)dihydrofuran-2(3H)-one; and,3-heptanoyl-4-(hydroxymethyl)dihydrofuran-2(3H)-one.
 10. A method ofimproving a yield of a microbially-produced bioactive secondarymetabolite product, the method comprising contacting cells of at leastone strain of microorganism with a suitable amount of at least oneγ-butyrolactone (GBL) composition wherein the GBL is non-cognate to thestrain or is synthetic and non-naturally occurring, and culturing thecells of the strain with the GBL under conditions for production of theproduct; and, obtaining the product from the cells by separation ofcells and medium or purification of the product from the cells andanalyzing the amount of the product, wherein the yield of the productper unit of volume of culture or weight of cells is greater than thatfrom control cells of the strain not contacted with the GBL compositionand otherwise identically cultured and analyzed, wherein the yield ofthe product from the cells cultured with the derivative of the GBL isimproved compared to that from the control cells.
 11. The methodaccording to claim 10, wherein the strain of microorganism is bacterial.12. The method according to claim 11, wherein the strain of bacteria isan actinomycete.
 13. The method according to claim 10, wherein thestrain of microorganism is fungal or algal.
 14. The method according toclaim 10 wherein the derivative of the GBL is synthetic andnon-naturally occurring and is at least one of the compositions selectedfrom formulas I-VI in FIG. 10 .
 15. The method according to claim 12,wherein a genus of the actinomycete selected from the group of generaconsisting of: Actinopolyspora, Amycolatopsis, Micromonospora, Nocardia,Pseudonocardia, Saccharothrix, Saccharopolyspora, Salinospora,Streptomyces, Tetinomedara, and Verrucosispora.
 16. The method accordingto claim 10, wherein the yield of the product from the cells contactedwith the GBL is at least about two-fold great, four-fold great, ten-foldgreater, or at least about twenty-fold greater than from the controlcells.
 17. The method according to claim 15, wherein the genus isStreptomyces and the species is selected from at least one of the groupconsisting of: avermitilis, S. aureofaciens, S. capreolus, S. cattleya,S. clavuligerus, S. coelicolor, S. ,fradiae, S. garyphallus, S. griseus,S. kanamyceticus, S. levoris, S. lincolnensis, S. niveus, S. noursei, S.platensis, S. plicatus, S. pristinaespiralis, S. orientalis, S.ribosidifus, S. rimosus, S. roseosporus, S. scabiei, S. venezuelae, S.vinaceus, and S. virginiae; or is at least one Pseudonocardia selectedfrom the group of: P. acacia; P. ailaonensis; P. adelaidensis; P.alaniniphila; P. ammonioxydans; P. carboxydivorans; P. halophobia; P.kujensis; P. nitrificans; P. petroleophila; P. salamisensis; P.sulfoxidans; P. thermophila; and P. zigingensis; or is at least oneAmycolatopsis selected from the group of: A. alba, A. azurea, S.balhimycena, A. coloradensis, A. fastidiosa, A. keratiniphila, A.lurida, A. mediterranei, A. orientalis, A. sulphurea, A. tolypomycina,and A. vancoresmycina.
 18. A method of discovery of a cell-producedsecondary metabolic compound in a microbial strain containing putativeunexpressed or under expressed genes encoding enzymes for biosynthesisof a chemical entity having a medicinal or industrial biologicalactivity, the method comprising: contacting cell samples containingcells from at least one microbial strain with at least one syntheticγ-butyrolactone (GBL) in an amount suitable for inducing secondarymetabolite expression, wherein the microbial strains are selected fromthe group of: fresh isolates from nature, a naturally occurring mixtureof unpurified microorganisms, and an established species strain whereinthe GBL and the established species are non-cognate; culturing the cellsamples with the GBL derivative under conditions for production of thesecondary metabolite chemical compounds; screening the cultures by atleast one detection system for presence of the biological activity, orby at least one detection system for presence of the metabolite not soexpressed in control samples not contacted with the GBL and otherwiseidentical and further screening the metabolite for the biologicalactivity, wherein the presence of the biological activity identifies theproducing sample containing at least one strain of microorganismproducing the chemical having the activity; and, characterizing at leastone chemical structure having the biological activity, and comparing thestructure to a library database of known chemical entities to obtainchemicals not previously known, thereby screening to discover thechemical compounds with the biological activity.
 19. The methodaccording to claim 18, wherein the at least one microbial straincontains at least two, at least five, or at least 10 strains.
 20. Themethod according to claim 18, wherein the GBL is a plurality of GBLshaving non-identical chemical structures, and the plurality is at leastfive GBLs.
 21. The method according to claim 20, wherein thenon-identical chemical structure comprises GBLs which are racemates,enantiomers, stereoisomers, or a racemic mixture.
 22. The methodaccording to claim 18, wherein screening further comprises contactingeach of the samples to the detection system for the biological activity,the detection system comprising at least one component selected from thegroup of: an enzyme, an organism, a tissue culture, a cell culture; themethod further comprising measuring an activity selected from:anti-bacterial, anti-fungal, anti-viral, anti-helminthic, anti-cancer,anti-malarial, anti-trypanosomal, complement inhibitory, immunestimulant, anti-inflammatory, toxin neutralizing, immune suppressant,diuretic, and herbicidal.
 23. The method according to claim 18, whereinculturing cell samples is in a liquid medium, and the method furthercomprises prior to screening, separating the cells from the medium toobtain a resulting supernatant depleted of the cells and a resultingcell pellet.
 24. The method according to claim 18, wherein culturingcell samples is in contact with soil, and the method further comprisesprior to screening, separating the cells from the soil and washing thesoil and cells, to obtain resulting components of supernatant, cellpellet, and soil, and assaying each for amount of the biologicalactivity.
 25. The method according to claim 18, further comprising afteridentifying, isolating the chemical compound from the producing culturecontacted with the GBL.
 26. The method according to claim 23, furthercomprising isolating, from the plurality of GBLs contacted to thesample, the at least one GBL that induces expression of the product. 27.The method according to claim 16, wherein characterizing the chemicalstructure further comprises analyzing by at least one method selectedfrom the group consisting of: mass spectrometry (MS); gaschromatography; thin layer chromatography; matrix-assisted laserdesorption/ionization (MALDI); MALDI-time of flight (MALDI-TOF); movingbed chromatography; and high performance liquid chromatography (HPLC).28. The method according to claim 20, wherein culturing is growth of thestrain or strains on solid medium, and screening further comprisesadding cells of a target indicator strain comprising at least one of abacterium, a fungus, a eukaryotic cell, a white blood cell, and aeukaryotic tissue explant.
 29. The method according to claim 26, whereinthe method further comprises testing a sample of the supernatant in atest subject which is an experimental animal model of a disease.
 30. Themethod according to claim 26, wherein the method further comprisestesting a sample of the supernatant in vivo in cultured cells or tissuesof an organism selected from the group consisting of: a mammal; afungus; a helminth; a plant; and, an insect.
 31. The method according toclaim 16, further comprising obtaining coordinates of peaks observed byMS, MALDI, MALDI-TOF, or HPLC corresponding to presence of secondarymetabolism products, and comparing the location of the peaks to that ofknown previously characterized products to identify chemical entities.32. The method according to claim 31 further comprising isolating andscreening the cell sample strains for production of the novel chemicalentities in presence of the GBL.
 33. A method of increasing oraccelerating production of a microbial secondary metabolism compound bya producing microorganism, the method comprising: contacting a cultureof the producing microorganism strain with a GBL at an effective dose toupregulate expression of genes encoding enzymes that synthesize thecompound, wherein the GBL is non-cognate to the strain.
 34. The methodaccording to claim 33, wherein the GBL is added at or before inoculationof production culture medium cells of the strain.
 35. The methodaccording to claim 33, wherein the GBL is added after inoculation orduring growth of cells of the strain.
 36. The method according to claim33, wherein the GBL is added at stationary phase or after cessation ofgrowth of the cells of the strain.
 37. The method according to claim 33,wherein the GBL is added at a plurality of time points during culture ofthe micro-organism.
 38. The method according to claim 33, furthercomprising comparing amount of the secondary metabolism compound withthat of a control culture not contacted with the GBL and otherwiseidentical.
 39. The method according to claim 33, wherein the effectivedose of the GBL is about 0.2 μM-0.8 μM, 0.8 μ-20 μM-100 μM, or isgreater than 100 μM.
 40. A chemical entity produced by a culture of S.coelicolor treated with at least one enantiomer or stereoisomer of3-(1-hydroxyheptyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one, and elutingfrom an analysis of an extract of the culture from a mass spec time offlight chromatogram at a peak at 1.84.